HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233196del , CM000667.2:g.55233196del | GRCh38 |
NC_000005.9:g.54529024del , CM000667.1:g.54529024del | GRCh37 |
NC_000005.8:g.54564781del | NCBI36 |
NG_034201.1:g.5523del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.329del MANE Select | ENSP00000282572.4:p.Lys110ArgfsTer19 | |
ENST00000282572.4:c.329del | ENSP00000282572.4:p.Lys110ArgfsTer19 | |
ENST00000501463.2:c.329del | ENSP00000422485.1:p.Lys110ArgfsTer19 | |
NM_021147.4:c.329del | NP_066970.3:p.Lys110ArgfsTer19 | |
NR_125346.1:n.523del | ||
NR_125347.1:n.523del | ||
NM_021147.5:c.329del MANE Select | NP_066970.3:p.Lys110ArgfsTer19 | |
NR_125346.2:n.414del | ||
NR_125347.2:n.414del |